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Kidney tissue regeneration using bioactive scaffolds incorporated with differentiating extracellular vesicles and intermediate mesoderm cells

Title
Kidney tissue regeneration using bioactive scaffolds incorporated with differentiating extracellular vesicles and intermediate mesoderm cells
Authors
Cha, Seung-Gyu; Rhim, Won-Kyu; Kim, Jun Yong; Lee, Eun Hye; Lee, Seung Yeon; Park, Jeong Min; Lee, Jeoung Eun; Yoon, Hyeji; Park, Chun Gwon; Kim, Bum Soo; Kwon, Tae Gyun; Lee, Youngmi; Lee, Dong Ryul; Han, Dong Keun
Ewha Authors
이영미
SCOPUS Author ID
이영미scopus
Issue Date
2023
Journal Title
BIOMATERIALS RESEARCH
ISSN
1226-4601JCR Link

2055-7124JCR Link
Citation
BIOMATERIALS RESEARCH vol. 27
Keywords
Kidney tissue regeneration; PMEZ scaffold; Intermediate mesoderm (IM); Differentiating extracellular vesicle (dEV); Kidney differentiation
Publisher
AMER ASSOC ADVANCEMENT SCIENCE
Indexed
SCIE; SCOPUS; KCI WOS scopus
Document Type
Article
Abstract
Background To overcome the limitations of current alternative therapies for chronic kidney disease (CKD), tissue engineering-mediated regeneration strategies have demonstrated the possibilities for complete kidney tissue regeneration. Given the challenges associated with the reproducibility of renal basal cells, the incorporation of intermediate mesoderm (IM) cells and bioactive materials to control bioactivities of cells with supported scaffolds should be considered as a viable approach to enable the regeneration of the complex kidney structure via renal differentiation. Methods We developed PMEZ scaffolds by combining crucial bioactive components, such as ricinoleic acid-grafted Mg(OH)2 (M), extracellular matrix (E), and alpha lipoic acid-conjugated ZnO (Z) integrated into biodegradable porous PLGA (P) platform. Additionally, we utilized differentiating extracellular vesicles (dEV) isolated during intermediate mesoderm differentiation into kidney progenitor cells, and IM cells were serially incorporated to facilitate kidney tissue regeneration through their differentiation into kidney progenitor cells in the 3/4 nephrectomy mouse model. Results The use of differentiating extracellular vesicles facilitated IM differentiation into kidney progenitor cells without additional differentiation factors. This led to improvements in various regeneration-related bioactivities including tubule and podocyte regeneration, anti-fibrosis, angiogenesis, and anti-inflammation. Finally, implanting PMEZ/dEV/IM scaffolds in mouse injury model resulted in the restoration of kidney function. Conclusions Our study has demonstrated that utilizing biodegradable PLGA-based scaffolds, which include multipotent cells capable of differentiating into various kidney progenitor cells along with supporting components, can facilitate kidney tissue regeneration in the mouse model that simulates CKD through 3/4 nephrectomy.
DOI
10.1186/s40824-023-00471-x
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자연과학대학 > 화학·나노과학전공 > Journal papers
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